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2902-96-7

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2902-96-7 Usage

Description

2-Nitro-1-propanol is an organic compound with the molecular formula C3H7NO3. It is a colorless to pale yellow liquid with a nitro group (-NO2) attached to the second carbon atom of a propane molecule. 2-NITRO-1-PROPANOL is known for its antimicrobial properties and its ability to inhibit methane production during in vitro ruminal fermentation.

Uses

Used in Chemical Synthesis:
2-Nitro-1-propanol is used as an intermediate in the improved synthesis of 2,2,2-trinitroethyl ethers. These ethers have various applications in the chemical industry, including the production of explosives and propellants.
Used in Animal Feed Industry:
2-Nitro-1-propanol is used as an antimicrobial supplement in the animal feed industry. It helps reduce the carriage of certain food-borne pathogens in animals, thereby improving the safety and quality of meat and dairy products.
Used in Environmental Applications:
2-Nitro-1-propanol is used to inhibit methane production during in vitro ruminal fermentation. This property makes it a valuable tool in the effort to reduce greenhouse gas emissions from livestock, as methane is a potent contributor to global warming.

Check Digit Verification of cas no

The CAS Registry Mumber 2902-96-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,0 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2902-96:
(6*2)+(5*9)+(4*0)+(3*2)+(2*9)+(1*6)=87
87 % 10 = 7
So 2902-96-7 is a valid CAS Registry Number.
InChI:InChI=1/C3H7NO3/c1-3(2-5)4(6)7/h3,5H,2H2,1H3/t3-/m1/s1

2902-96-7 Well-known Company Product Price

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  • Alfa Aesar

  • (43843)  2-Nitro-1-propanol, 97%   

  • 2902-96-7

  • 5g

  • 351.0CNY

  • Detail
  • Alfa Aesar

  • (43843)  2-Nitro-1-propanol, 97%   

  • 2902-96-7

  • 25g

  • 2226.0CNY

  • Detail
  • Alfa Aesar

  • (43843)  2-Nitro-1-propanol, 97%   

  • 2902-96-7

  • 100g

  • 3334.0CNY

  • Detail

2902-96-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-nitropropan-1-ol

1.2 Other means of identification

Product number -
Other names 2-Nitropropanol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2902-96-7 SDS

2902-96-7Relevant articles and documents

Synthesis and spin trapping properties of polystyrene supported trifluoromethylated cyclic nitrones

Earla, Aruna,Walter, Eric D.,Braslau, Rebecca

, p. 1084 - 1100 (2019)

Polystyrene supported fluorinated cyclic nitrone spin-traps: Resin-2-HFDMPO (2-hydroxymethyl-2-methyl-5-(trifluoromethyl)-3,4-dihydro-2H-pyrrole-1-oxide) and Resin-2-PFDMPO (2-(3-hydroxypropyl)-2-methyl-5-(trifluoromethyl)-3,4-dihydro-2H-pyrrole 1-oxide) containing a trifluoromethyl pyrroline-N-oxide core were developed to detect free radicals under flow conditions. A continuous flow EPR technique was used to evaluate the spin trapping properties of these tethered nitrones. While both resins trapped radicals, polymer supported nitrone Resin-2-PFDMPO with a longer and more flexible linker showed a more information rich spectrum than Resin-2-HFDMPO.

Erratum: Catalytic enantioselective protonation of nitronates utilizing an organocatalyst chiral only at sulfur (Journal of the American Chemical Society (2012) 134 (9058-9061)DOI: 10.1021/ja3026196)

Kimmel, Kyle L.,Weaver, Jimmie D.,Lee, Melissa,Ellman, Jonathan A.

supporting information; experimental part, p. 11828 - 11828 (2012/09/07)

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Polyamine alcohol derivatives

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Page/Page column 3-4, (2012/07/03)

A compound having formula (I) wherein R1 is methyl or ethyl; R2 is hydrogen, methyl, CH2C(NH2)(R1)(CH2OH) or R2 groups combine to form a difunctional C2-C6 alkyl group; and X is a difunctional group selected from the group consisting of C2-C20 alkyl, C5-C20 cycloalkyl, C6-C10 aryl, C8-C20 aryl alkyl, C4-C20 heteroalkyl or C10-C20 aryl heteroalkyl.

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